Your English writing platform
Discover LudwigSuggestions(1)
Exact(1)
After elution with 20 µl 2× SDS loading buffer, proteins were resolved by SDS-PAGE and analyzed by Western blotting with anti-HA antibody to detect ubiquitination, and anti-WRN antibody to detect WRN protein level.
Similar(59)
After the final wash, the pellet was resuspended in sample buffer, and proteins were resolved by SDS-PAGE (4 12% Bis-Tris NuPAGE gel) and transferred to a PDVF membrane for immunoblot analysis using HRP-conjugated V5 or Myc antibodies.
The pellet was resuspended in a 2x Laemmli sample buffer and proteins were resolved by SDS-PAGE and immunoblotted forBcl-2 and Bcl-xL as above.
Beads were mixed with 30 µl of Laemmli blue buffer, and proteins were resolved on a 12 SDS-PAGE and transferred onto PVDF transfer membrane.
Pellets and supernatants were mixed with Laemmli blue buffer and proteins were resolved on a 12% SDS-PAGE and transferred onto PVDF transfer membrane.
Reactions were stopped by adding 5X sample buffer, and proteins were resolved by SDS-PAGE.
Beads were boiled in sample loading buffer and proteins were resolved on a reducing SDS-PAGE gel.
Bound gephyrins were released by boiling in SDS‐loading buffer, and proteins were resolved on a 6% SDS PAGE.
The dried material was dissolved in 10 μl loading buffer, and proteins were resolved by SDS-PAGE on 14% polyacrylamide gel for 250 Vh.
Bacterial pellets recovered after inductions were dissolved in appropriate volume of Laemmli buffer and proteins were resolved on a 12% SDS-PAGE.
Elution was performed using Laemmli buffer, and proteins were resolved on SDS-PAGE, followed by western blotting analysis with appropriate antibodies.
Write better and faster with AI suggestions while staying true to your unique style.
Since I tried Ludwig back in 2017, I have been constantly using it in both editing and translation. Ever since, I suggest it to my translators at ProSciEditing.

Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com